HEMOCLAV VENOUS CATHETER— 510(k) K831801

Substantially Equivalent

Exo, Inc.

FDA 510(k) clearance K831801 for HEMOCLAV VENOUS CATHETER, Substantially Equivalent on 1983-07-07. Applicant: Exo, Inc..

Clearance details

Applicant: Exo, Inc.
Product code: Code FIQ
Advisory panel: Gastroenterology, Urology
Date received: 1983-06-03
Decision date: 1983-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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